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Click Mono-Azido-Nanogold® 1.4 nm

Click chemistry with covalently bound Nanogold® labels! Reacts with alkynes, copper-catalyzed (CuAAC) or copper-free (SPAAC).

Nanoparticle Size: 1.4 nm
Reactive Groups: CLICK Azide
Unit Sizes: 6 nmol x 5, 6 nmol, 30 nmol

Click Mono-Azido-Nanogold® 1.4 nm

Click chemistry with covalently bound Nanogold® labels! Reacts with alkynes, copper-catalyzed (CuAAC) or copper-free (SPAAC).

Nanoparticle Size: 1.4 nm
Reactive Groups: CLICK Azide
Unit Sizes: 6 nmol x 5, 6 nmol, 30 nmol
SKU
Description
Price
  • 2026S-6NMOL

Unit Size: 6 nmol

$ 173.00

  • 2026A-5X6NMOL

Unit Size: 6 nmol x 5

$ 610.00

  • 2026-30NMOL

Unit Size: 30 nmol

$ 547.00

Our Nanogold® labeling reagents are also available in:

Grow the size - Keep the precision

Combine nanoparticle developers with Nanogold® labels

Easy, archival developers for any scope or blots
  • GoldEnhance™:
    Simple. Superior. Precision nanoparticle enhancement
    Sharp, archival staining of blots or easy viewing in any scope.
  • Silver Enhancement:
    Precision nanoparticles, not colloidal silver blobs: precise development for any scope.
Product Information

Click Mono-Azido-Nanogold® 1.4 nm

Precision Nanogold® labels for Click chemistry!

Click chemistry is the reaction between an azide and an alkyne or similar group. It is a bio-orthogonal reaction (i.e. it does not occur naturally) which lets let you label selectively in living cells, tissues and even animals without cross-reactivity.

Three different reactivities are available to let you label both alkyne-modified and azide-modified targets using copper-catalyzed (CuAAC) or copper-free (SPAAC) reactions:

  • 1.4 nm Mono-Azido Nanogold® reacts with alkynes and related reagents; may be used for copper-catalyzed (CuAAC) or copper-free (SPAAC) click reactions.
  • 1.4 nm Mono-Alkyne Nanogold® reacts with azides via copper-catalyzed (CuAAC) reaction.
  • 1.4 nm Mono-DBCO-Nanogold® reacts with azides via copper-free SPAAC reaction.
Click-Nanogold® labeling: Combine the power of click chemistry with the precision of our famous gold nanoparticles. Choose from Azide, Alkyne and DBCO.

Applications:

  • Label dynamic processes in living cells or tissues – Click reagents will not hydrolyze or degrade.
  • Label components in living cells: do not react with endogenous species like biotin or cross-reactive proteins.
  • High-resolution labeling of subunits or molecular sites: just incorporate the corresponding reactive azide or alkyne into the target – no antibody or probe required.
  • Optical Visualization: use silver or gold enhancement to visualize by light microscopy or for super-sensitive blotting. See as little as 1 pg of target IgG!
  • Multiplex your labeling: Add a click reaction to detect an additional target if there is no suitable antibody or probe.

1.4 nm Nanogold® Labeling Reagents

Nanogold® is a better gold label.

The 1.4 nm Nanogold® particle is a gold compound: it is not just adsorbed to proteins, like colloidal gold, but covalently reacts at specific sites under mild buffer conditions. This gives a well defined product that can be purified chromatographically.

Nanogold® brings the versatility of fluorescent conjugation to gold labeling.

Label virtually any molecule

Label any molecule with a suitable reactive group: oligonucleotides, lipids, peptides, proteins, enzyme inhibitors and others. This is a big improvement over colloidal gold, which may be adsorbed only to antibodies and a limited range of proteins and peptides.

Nanogold® is small and highly uniform in size, in sharp contrast to small colloidal gold preparations (most commonly used “1 nm” colloidal golds actually range from 1 to 3 nm).

Label your own biomolecules with our Nanogold® labeling reagents,
or check out our range of antibody IgG, Fab’ and streptavidin Conjugates with Nanogold®.

Left: Silver-enhanced Nanogold®-labeled K+ channel Kv2.1 subunit in rat brain, X15,000 (J.-H. Tao-Cheng, NIH). Right: Darkfield STEM micrographs of Maleimido Nanogold® labeled A β peptide targeting proteasomes; sample was stained with methylamine vanadate. White dots are 1.4 nm Nanogold®. From Gregori, L., Hainfeld, J.F., Simon, M.N., and Goldgaber, D. (1997). Binding of amyloid beta protein to the 20S proteasome. J. Biol. Chem. 272, 58-62.

Left: Silver-enhanced Nanogold®-labeled K+ channel Kv2.1 subunit in rat brain, X15,000 (J.-H. Tao-Cheng, NIH).
Right: Darkfield STEM micrographs of Maleimido Nanogold® labeled A β peptide targeting proteasomes; sample was stained with methylamine vanadate. White dots are 1.4 nm Nanogold®.

From Gregori, L., Hainfeld, J.F., Simon, M.N., and Goldgaber, D. (1997). Binding of amyloid beta protein to the 20S proteasome. J. Biol. Chem. 272, 58-62.

Easily enhanced for electron microscopy, light microscopy, cryo-EM, blots…

Try our precision nanoparticle developers for slow development with low background!

Features and Advantages

  • Unparalleled penetration of conjugates -up to 40 µm!
  • Higher density of immunolabeling than with larger gold probes.
  • Can be conjugated to any molecule with a suitable reactive group. Available with different reactivities.
  • Extremely uniform 1.4 nm gold particle.
  • Label at specific sites which do not obstruct native reactivity.
  • Close to stoichiometric labeling.
  • Reacts under mild, neutral conditions.
  • Conjugates are easily isolated by gel filtration.
  • Conjugates are stable to a wide range of pH and ionic strengths.
  • High stability: conjugates show unchanged reactivity after storage for a year.
Nanogold® labels only at specific reactive sites. Labeling is selective for thiols (cysteine residues) or primary amines (N-terminal, lysine residues).